FDA Adverse Event Malfunction Summary report: N

8024190

MDR report key: 8024190 · Received October 31, 2018

Report

Report Number
8024190
Event Type
Malfunction
Date Received
October 31, 2018
Date of Event
October 22, 2018
Report Date
October 26, 2018
Product Problem
Yes
Report Source
User Facility report
Reporter Location
FL
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

SKIN PEELING WAS NOTED ON LEFT MEDIAL THIGH WHEN THE DRAPES/IOBAN WAS PULLED OFF. SKIN TEAR NOTED ON THE RIGHT SCAPULA FROM THE R2 PAD SITE WHEN PADS WERE TAKEN OFF. MANUFACTURER'S GUIDELINES WERE FOLLOWED WHEN TAKING OFF R2 PADS. THERE WAS SLOUGHING OF SKIN ON LEFT INNER THIGH WITH REGARD DEFIBRILLATOR PADS.

Patients

Seq Age Sex Outcome Treatment
1 25185 DA Other